Homo sapiens mRNA for FLJ00010 protein, partial cds

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Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorder. [Genet Med. 2024]
Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorder.
Accogli A, Park YN, Lenk GM, Severino M, Scala M, Denecke J, Hempel M, Lessel D, Kortüm F, Salpietro V, et al. Genet Med. 2024 May; 26(5):101097. Epub 2024 Feb 5.
Clinical value of SLC12A9 for diagnosis and prognosis in colorectal cancer. [Aging (Albany NY). 2023]
Clinical value of SLC12A9 for diagnosis and prognosis in colorectal cancer.
Du W, Xia G, Chen L, Geng L, Xu R, Han Q, Ying X, Yu H. Aging (Albany NY). 2023 Dec 28; 15(24):15419-15433. Epub 2023 Dec 28.
Upregulation of SLC12A3 and SLC12A9 Mediated by the HCP5/miR-140-5p Axis Confers Aggressiveness and Unfavorable Prognosis in Uveal Melanoma. [Lab Invest. 2023]
Upregulation of SLC12A3 and SLC12A9 Mediated by the HCP5/miR-140-5p Axis Confers Aggressiveness and Unfavorable Prognosis in Uveal Melanoma.
Yan C, Hu X, Liu X, Zhao J, Le Z, Feng J, Zhou M, Ma X, Zheng Q, Sun J. Lab Invest. 2023 Mar; 103(3):100022. Epub 2023 Jan 10.

RefSeq alternative splicing
See 21 reference mRNA sequence splice variants for the SLC12A9 gene.

dual specificity protein phosphatase CDC14B isoform X12 [Homo sapiens]
dual specificity protein phosphatase CDC14B isoform X12 [Homo sapiens]
gi|2462627018|ref|XP_054220057.1|

Protein
Homo sapiens arginine/serine-rich coiled-coil 1, mRNA (cDNA clone MGC:12197 IMAG...
Homo sapiens arginine/serine-rich coiled-coil 1, mRNA (cDNA clone MGC:12197 IMAGE:3997840), complete cds
gi|13937768|gb|BC006982.1|

Nucleotide

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Nucleotide